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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 391408Erstellt: 25. Oktober 2026

Triphenylphosphine → 3-(Bromomethyl)-5-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/391408

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktN-bromobutanimideHCID 67184—
Edukt3-(Hydroxymethyl)-5-(trifluoromethyl)benzonitrileHCID 11701221—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(Bromomethyl)-5-(trifluoromethyl)benzonitrileHCID 11601369—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3-(Hydroxymethyl)-5-(trifluoromethyl)benzonitrile (0.33 mg, 1.64 mmol) and triphenylphosphine (0.86 g, 3.28 mmol) were combined in methylene chloride (6 mL) and cooled to 0° C. N-Bromosuccinimide (0.61 mg, 3.43 mmol) was introduced in portions and the reaction allowed to warm to room temperature. After 16 h, the reaction mixture was diluted with methylene chloride, washed with concentrated sodium bicarbonate (2×), brine (2×), dried over sodium sulfate, and concentrated. Column chromatography on silica gel (20% ethyl acetate/hexanes) gave 0.36 g (83%). 1H-NMR (CDCl3, 500 MHz) δ 7.97 (s, 2H), 7.84 (s, 1H), 4.50 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08383821B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-7e23b24fbf744967ae3683bf41d8c9a8
Quellennotizuspto-grants-2013_02